A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9753777



Internal ID18728023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:9277714..9277818hg38UCSC Ensembl
Outerchr18:9277706..9277832hg38UCSC Ensembl
Innerchr18:9277712..9277816hg19UCSC Ensembl
Outerchr18:9277704..9277830hg19UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg38127
hg19127
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3555030
Supporting Variants
Samples
Known GenesANKRD12
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9753777
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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